RSPP guidance documents
The following documents provide guidance on various topic and issues pertaining to research with human subjects. Please contact the RSPP office for further information.
- Ensuring Effective and Legal Informed Consent in Clinical Research
- Application for Continuing Review/Final Report
- Enrolling Non-English Speaking Research Subjects
- Informed Consent Language for Medications that Commonly Cause Drowsiness
- Using Mental Health Records for Research Purposes
- Research Protocols and Suicide Risks
- Research Protocols and Deception
- RSPP Call Guidance
- Local Event Reporting Summary Memo
- External Event Reporting Summary Memo
- Conflict of Interest
- Caregiver Information Sheet and ICF Guidance Document
- Guidance Conducting Investigator-Initiated Multisite Collaborative Research
- FDA Guidance on Conflicts of Interest
